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MyLab XPro30

EUDAMED

Class IIa (EU MDR)

Ref 101740007Model 7400

by Esaote S.p.A.

Identity

Trade Name
MyLab XPro30 EUDAMED
Model / Reference
7400 EUDAMED
101740007 EUDAMED

Identifiers

Primary DI / UDI-DI
08056304454201 EUDAMED
Basic UDI-DI
805630445ESA.US0000005.Y7 EUDAMED
B-08056304454201 EUDAMED
EMDN Code
Z11040103 PORTABLE ULTRASOUND SCANNERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

MyLab XPro30 by Esaote S.p.A. — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Esaote S.p.A.
EUDAMED SRN
IT-MF-000019024

Sources (2)

  • EUDAMED c12ac1c5-78df-4817-a17b-ca439fcf899c 61 fields · synced Jul 10, 2026
  • EUDAMED 5a6e52ed-0d26-4883-914c-f3c74db45abd 61 fields · synced May 17, 2026